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Hyperinflation

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Hyperinflation FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
Disposable Hyperinflation System, 1/2L Breathing Bag (Latex Free), 7' O2 and Pressure Lines, Series 900 Infant Mask FDA UDI
Model / Reference
7-N7905-I FDA UDI
Description
Disposable Hyperinflation System, 1/2L Breathing Bag (Latex Free), 7' O2 and Pressure Lines, Series 900 Infant Mask FDA UDI

Identifiers

Primary DI / UDI-DI
00709078063855 FDA UDI
510(k) Number
K932709 FDA UDI
FDA Product Code
BZR FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ventilator breathing circuit, single-use

Hyperinflation by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI c5cf78a2-0ed8-441e-9dac-ebb4d6d17820 34 fields · synced Jun 1, 2026